National Clinical Research Center for Child Health of the Children's Hospital, Zhejiang University School of Medicine, Hangzhou, 310058 Zhejiang, P.R. China; Columbia Center for Human Development & Division of Digestive and Liver Disease, Department of Medicine, Columbia University Medical Center, NY 10032, USA.
Columbia Center for Human Development & Division of Digestive and Liver Disease, Department of Medicine, Columbia University Medical Center, NY 10032, USA.
Dev Cell. 2021 Jun 7;56(11):1646-1660.e5. doi: 10.1016/j.devcel.2021.04.027. Epub 2021 May 18.
Mucus-secreting goblet cells are the dominant cell type in pulmonary diseases, e.g., asthma and cystic fibrosis (CF), leading to pathologic mucus metaplasia and airway obstruction. Cytokines including IL-13 are the major players in the transdifferentiation of club cells into goblet cells. Unexpectedly, we have uncovered a previously undescribed pathway promoting mucous metaplasia that involves VEGFa and its receptor KDR. Single-cell RNA sequencing analysis coupled with genetic mouse modeling demonstrates that loss of epithelial VEGFa, KDR, or MEK/ERK kinase promotes excessive club-to-goblet transdifferentiation during development and regeneration. Sox9 is required for goblet cell differentiation following Kdr inhibition in both mouse and human club cells. Significantly, airway mucous metaplasia in asthmatic and CF patients is also associated with reduced KDR signaling and increased SOX9 expression. Together, these findings reveal an unexpected role for VEGFa/KDR signaling in the defense against mucous metaplasia, offering a potential therapeutic target for this common airway pathology.
黏液分泌杯状细胞是肺部疾病(如哮喘和囊性纤维化(CF))中的主要细胞类型,导致病理性黏液化生和气道阻塞。包括 IL-13 在内的细胞因子是将棒状细胞转化为杯状细胞的主要因素。出乎意料的是,我们发现了一条以前未被描述的促进黏液化生的途径,该途径涉及 VEGFa 和其受体 KDR。单细胞 RNA 测序分析结合遗传小鼠模型表明,上皮细胞 VEGFa、KDR 或 MEK/ERK 激酶的缺失会促进发育和再生过程中棒状细胞向杯状细胞的过度转化。在 Kdr 抑制后,Sox9 是小鼠和人类棒状细胞中杯状细胞分化所必需的。重要的是,哮喘和 CF 患者的气道黏液化生也与 KDR 信号的降低和 SOX9 表达的增加有关。总之,这些发现揭示了 VEGFa/KDR 信号在防御黏液化生中的意外作用,为这种常见的气道病理提供了一个潜在的治疗靶点。